Evidence map›Paper›PMID 35158829›Full record

ArticleCancers2022

Development of Preclinical Ultrasound Imaging Techniques to Identify and Image Sentinel Lymph Nodes in a Cancerous Animal Model.

Marion Bacou, Vidya Rajasekaran, Adrian Thomson, Sandra Sjöstrand, Katarzyna Kaczmarek, Anna Maria Ochocka-Fox, Adam D Gerrard, Susan Moug, Tomas Jansson, Helen Mulvana and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 2 countries.

Marion BacouCancer Research UK Edinburgh Centre, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh EH4 2XR, UK.
Vidya RajasekaranCancer Research UK Edinburgh Centre, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh EH4 2XR, UK.
Adrian ThomsonCentre for Cardiovascular Science, University of Edinburgh, Edinburgh EH16 4JT, UK.ORCID 0000-0001-7320-300X
Sandra SjöstrandDepartment of Biomedical Engineering, Faculty of Engineering, Lund University, 223 63 Lund, Sweden.ORCID 0000-0001-5069-0968
Katarzyna KaczmarekBiomedical Engineering, University of Strathclyde, Glasgow G1 1QE, UK.ORCID 0000-0002-3193-0070
Anna Maria Ochocka-FoxMRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh EH4 2XR, UK.
Adam D GerrardMRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh EH4 2XR, UK.ORCID 0000-0001-5649-9240
Susan MougDepartment of Surgery, Royal Alexandra Hospital, Paisley PA2 9PJ, UK.
Tomas JanssonDepartment of Clinical Sciences Lund, Biomedical Engineering, Lund University, 223 63 Lund, Sweden.
Helen MulvanaBiomedical Engineering, University of Strathclyde, Glasgow G1 1QE, UK.
Carmel M MoranCentre for Cardiovascular Science, University of Edinburgh, Edinburgh EH16 4JT, UK.ORCID 0000-0002-2105-2948
Susan M FarringtonCancer Research UK Edinburgh Centre, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh EH4 2XR, UK.ORCID 0000-0001-5955-7389
Edinburgh Cancer Research · GBInstitute of Genetics and Cancer · GBLund University · SEUniversity of Edinburgh · GBUniversity of Strathclyde · GBRoyal Alexandra Hospital · GB

Funding

Cancer Research UK A23333Medical Research Council MR/K018647/1
6 · The paper itself

Abstract

Lymph nodes (LNs) are believed to be the first organs targeted by colorectal cancer cells detached from a primary solid tumor because of their role in draining interstitial fluids. Better detection and assessment of these organs have the potential to help clinicians in stratification and designing optimal design of oncological treatments for each patient. Whilst highly valuable for the detection of primary tumors, CT and MRI remain limited for the characterization of LNs. B-mode ultrasound (US) and contrast-enhanced ultrasound (CEUS) can improve the detection of LNs and could provide critical complementary information to MRI and CT scans; however, the European Federation of Societies for Ultrasound in Medicine and Biology (EFSUMB) guidelines advise that further evidence is required before US or CEUS can be recommended for clinical use. Moreover, knowledge of the lymphatic system and LNs is relatively limited, especially in preclinical models. In this pilot study, we have created a mouse model of metastatic cancer and utilized 3D high-frequency ultrasound to assess the volume, shape, and absence of hilum, along with CEUS to assess the flow dynamics of tumor-free and tumor-bearing LNs in vivo. The aforementioned parameters were used to create a scoring system to predict the likelihood of a disease-involved LN before establishing post-mortem diagnosis with histopathology. Preliminary results suggest that a sum score of parameters may provide a more accurate diagnosis than the LN size, the single parameter currently used to predict the involvement of an LN in disease.

Indexed as

3D ultrasoundcolorectal cancercontrast-enhanced ultrasoundlymph nodemetastatic mouse modelpreclinical

Identifiers

PMID35158829
PMCPMC8833694
OpenAlexW4212993054

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.